Results 281 to 290 of about 315,624 (316)
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Does VLDL‐LDL‐Cholesterol in Cord Serum Predict Future Level of Lipoproteins?
Acta Paediatrica, 1991ABSTRACT. Lipoproteins were measured in 618 healthy, full‐term newborns. Seventy‐four with a VLD‐LDL‐cholesterol above 1.3 mmol/l (50 mg/dl) at birth and 25 randomly chosen controls with VLDL‐LDL‐cholesterol l.3 mmol/l or below at birth were followed up at age 2.
V, Fønnebø +3 more
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VLDL compositional changes and plasma levels of triglycerides and high density lipoprotein
Clinica Chimica Acta, 1998VLDL chemical composition is related to plasma levels of triglycerides and HDL-cholesterol. We evaluated patients with primary hypertriglyceridemia with or without hypoalphalipoproteinemia and subjects with normotriglyceridemia with hypoalphalipoproteinemia.
F D, Brites +6 more
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Normal VLDL metabolism despite altered lipoprotein composition in type 1 diabetes mellitus
Clinical Endocrinology, 2001OBJECTIVES Patients with type 1 diabetes are at increased risk of cardiovascular disease, which may be related to abnormal lipid metabolism. Secretion and clearance of VLDL apolipoprotein B100 (apoB) are important determinants of plasma lipid concentrations and are known to be influenced by hormones, including insulin and growth hormone.PATIENTS This ...
Christ, E R +8 more
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Effect of increased afterload on cardiac lipoprotein lipase and VLDL receptor expression
Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids, 1999Fatty acids are a major source of fuel for energy production by myocytes. Lipoprotein lipase (LPL) and very low density lipoprotein (VLDL) receptor are abundantly expressed by the heart and skeletal muscles. LPL and possibly VLDL receptor represent the primary route of access to fatty acids contained in circulating triglyceride-rich lipoproteins ...
N D, Vaziri, K, Liang, C H, Barton
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Species differences of macrophage very low-density-lipoprotein (VLDL) receptor protein expression
Biochemical and Biophysical Research Communications, 2011Triglyceride-rich lipoproteins (TGRLs) and low-density-lipoprotein (LDL) cholesterol are independent risk factors for coronary artery disease. We have previously proposed that the very low-density-lipoprotein (VLDL) receptor is one of the receptors required for foam cell formation by TGRLs in human macrophages.
Sadao, Takahashi +13 more
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Biochemical and Biophysical Research Communications, 1984
Lipolysis of human very low density lipoproteins (VLDL) by lipoprotein lipase (LPL) was inhibited in the presence of high density lipoproteins (HDL), anti-apolipoprotein (apo) CII, and by increasing the VLDL free cholesterol content but not with anti-apo CIII or lipoprotein-free plasma.
B W, Liu, B A, Hynd, M L, Kashyap
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Lipolysis of human very low density lipoproteins (VLDL) by lipoprotein lipase (LPL) was inhibited in the presence of high density lipoproteins (HDL), anti-apolipoprotein (apo) CII, and by increasing the VLDL free cholesterol content but not with anti-apo CIII or lipoprotein-free plasma.
B W, Liu, B A, Hynd, M L, Kashyap
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The Lipoproteins and Arterial Smooth Muscle Cells: Uptake of VLDL, LDL, HDL
1977Serum lipoproteins are considered the main source of cholesterol of “peripheral” cells and studies with perfused aorta have shown that human LDL and HDL can cross normal aortic endothelium, most probably via the plasmalemmal vesicles (1). Thus even under normal conditions aortic smooth muscle cells are exposed to some serum lipoproteins, the presence ...
O, Stein, Y, Stein
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Experimental hematology, 1983
The organ distribution of very low density lipoproteins, with known hematopoietic cell growth inhibitory effects, was studied in the rat. Animals received intravenous injections of 125I-labelled VLDL and tissue uptake was monitored over 4 days. Uptake into 8 organs was studied using a technique that excluded blood associated radioactivity.
K, Cornetta, S, Zucker
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The organ distribution of very low density lipoproteins, with known hematopoietic cell growth inhibitory effects, was studied in the rat. Animals received intravenous injections of 125I-labelled VLDL and tissue uptake was monitored over 4 days. Uptake into 8 organs was studied using a technique that excluded blood associated radioactivity.
K, Cornetta, S, Zucker
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Scandinavian Journal of Clinical and Laboratory Investigation, 1975
K. Carlson, L. Carlson
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K. Carlson, L. Carlson
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